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المؤلفون: M, Hattori, A, Fujiyama, T D, Taylor, H, Watanabe, T, Yada, H S, Park, A, Toyoda, K, Ishii, Y, Totoki, D K, Choi, Y, Groner, E, Soeda, M, Ohki, T, Takagi, Y, Sakaki, S, Taudien, K, Blechschmidt, A, Polley, U, Menzel, J, Delabar, K, Kumpf, R, Lehmann, D, Patterson, K, Reichwald, A, Rump, M, Schillhabel, A, Schudy, W, Zimmermann, A, Rosenthal, J, Kudoh, K, Schibuya, K, Kawasaki, S, Asakawa, A, Shintani, T, Sasaki, K, Nagamine, S, Mitsuyama, S E, Antonarakis, S, Minoshima, N, Shimizu, G, Nordsiek, K, Hornischer, P, Brant, M, Scharfe, O, Schon, A, Desario, J, Reichelt, G, Kauer, H, Blocker, J, Ramser, A, Beck, S, Klages, S, Hennig, L, Riesselmann, E, Dagand, T, Haaf, S, Wehrmeyer, K, Borzym, K, Gardiner, D, Nizetic, F, Francis, H, Lehrach, R, Reinhardt, M L, Yaspo
المساهمون: Antonarakis, Stylianos
المصدر: Nature, Vol. 405, No 6784 (2000) pp. 311-319
مصطلحات موضوعية: ddc:616, Genetics, Multidisciplinary, Autosome, Base Sequence, Contig, Gene map, Chromosomes, Human, Pair 21, Molecular Sequence Data, Chromosome Mapping, Chromosome, DNA, Dna, Sequence Analysis, DNA, Genome project, Biology, Genes, Chromosome 19, Mutation, Humans, Down Syndrome, Chromosome 21, Chromosome 22, Down Syndrome/genetics
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2
المؤلفون: F. Pelliccia, M. Gerbault-Seureau, J. Daut, C. Denning, T. Meitinger, G. Fakis, K. Kikuchi, A. Dalski, H.G. Nothwang, N. Vogt, Y. Liu, M. Breen, P. Lichter, B. Malfoy, K.-H. Grzeschik, A. Rocchi, D. Incarnato, H.M. Mitchison, I. Papet, A.L. Loudon, C. Rossier, S. Schneider, B. Pedersen, D. Vogt, E. Chung, C. Menzel, L. Chen, G.A. Wittert, J. Perret, F. Willeke, L. Ferrara, Y. Watanabe, B. Ugele, W. Engel, V. Buckle, K.J. Fowler, S.E. Antonarakis, M.L. Ramírez-Dueñas, S.I. Anderson, M.E. Delany, R. Swanson, H. Turnbull, D. Sheer, T.E. Whitmore, F. Wei, M. Meeks, P. B. Bennett, H. Engel, A. Perucatti, J. Bonfils, A.C. Jelmberg, S.M. van der Maarel, K. Masuda, S. Lok, P.J. Hope, Y. Matsuda, L. French, R. Hawken, Ch. Zühlke, A. Hebinck, T. Lehnert, D.B. Zimonjic, R.H. Martin, E. Schwinger, R.M. Gardiner, M.L. Ayala-Madrigal, F. Liners, J.-P. Fryns, T.M. Skinner, T. Haaf, S.W. Scherer, M.M. Miller, E. Chevret, L. Rießelmann, R. Blevins, M.L. Watson, I.M. Adham, C.S. Haley, G.C. Webb, R. Shamsadin, M. Parmentier, L. Bartoloni, J. Koch, C. Gehrig, H. Hayes, S. Spiden, A.W.I. Lo, M.Z. Limongi, S. Ohl, S. Kollers, J.-L. Blouin, E. McKenna, A.B. Krupkin, J. Bernardino, D.S. Haines, J.L. Holloway, H.H. Ropers, R.M. Hope, C.E. Lofton-Day, A.R. Zinn, J. Wirth, S. Joos, N.C. Popescu, C. Lindbjerg Andersen, C.D. DeLozier-Blanchet, E.P. Cribiu, M. Østergaard, B. Brenig, E.V. Volpi, L. Schibler, B. Hinzmann, A. Krempler, M. Faure, M. Payton, N.K. Moschonas, A. Niveleau, N. Inoue, H.F. Otto, L. De Moerlooze, Q. Shi, B. Nielsen, P. Deloukas, K.H.A. Choo, M.F. Seldin, M. Otaño-Joos, C. Derst, D. Lefrançois, A. Schröer, I. Hansmann, P. Kalitsis, M.F. Maurer, R. Fries, M.T. Boyd, T.J. Quinton, A. Vilain, J.B. Vincent, K.K. Wilgenbus, G. von Beust, G.P. Di Meo, B. Dutrillaux, L. Gaddini, W. Scheurlen, G. Mechtersheimer, S. Doerr, A.L. Archibald, L. Iannuzzi, E. Sim, K. Regemann, R. Athwal, S. Kübart, A. Rosenthal, D.J. Figueroa, N. Tommerup, M.-G. Mattei, H. Shima, D.F.S. Longmuir, A.K. Maiti, J. Williamson, N.L. Lopez-Corrales, S. Boukouvala, C.P. Austin
المصدر: Cytogenetic and Genome Research. 90:154-168
مصطلحات موضوعية: medicine.medical_specialty, Anthropology, Genetics, Cytogenetics, medicine, Biology, Molecular Biology, Genetics (clinical)
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3
المؤلفون: B. Hinzmann, H.H. Ropers, S.M. van der Maarel, D Vogt, Silke Schneider, Jean-Pierre Fryns, Hans Gerd Nothwang, Corinna Menzel, S. Kübart, L Riesselmann, Niels Tommerup, J. Wirth, Andreas Schröer, André Rosenthal, Thomas Haaf
المصدر: Cytogenetic and Genome Research. 90:126-133
مصطلحات موضوعية: Adult, Male, X Chromosome, Adolescent, viruses, Population, Molecular cloning, Biology, Translocation, Genetic, Sequence-tagged site, Gene mapping, Dosage Compensation, Genetic, Intellectual Disability, Sequence Homology, Nucleic Acid, Genetics, Humans, RNA, Messenger, Cloning, Molecular, Child, education, Molecular Biology, In Situ Hybridization, Fluorescence, Genetics (clinical), X chromosome, Sequence Tagged Sites, Expressed Sequence Tags, Recombination, Genetic, education.field_of_study, Autosome, Reverse Transcriptase Polymerase Chain Reaction, Breakpoint, Infant, Chromosome Breakage, Exons, Physical Chromosome Mapping, Child, Preschool, Female, Chromosome breakage
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المؤلفون: D. Levanon, T.B. Shows, K. Pinchin, K.R. Sims, R.H. Martin, D.A. Collier, I.C. Scott, S. Aytay, B. Goldman, D. Job, H.T. Wong, K. L. Puschus, K.L. Chow, A.C. Clase, S.M. Bell, A. Siegel, P.B. Singh, P. Kools, M. Bullejos, J.P. Adelman, A.W. Rademaker, S. Wedgwood, Y. Gronera, J.P. Chapple, A. Aviram-Goldring, S.C. Kingswood, D. Motzkus, F. Ventura, M. Litt, C.T. Bond, C. Bosc, A.T. Kumamoto, A. Sánchez, T. Haaf, R. Jiménez, A.F. Markham, A.J. Hardcastle, H. Röck, T. Sawazaki, C. Vourc’h, R.L.Y. Wong, G. Barkai, M.E. Cheetham, P.L. Coletta, R.L. Eddy, L.M. Davis, R. Díaz de la Guardia, M. Aldaz, L. Riesselmann, M. Burgos, E. Navarro, C. Cruz, F. Van Roy, E. Denarier, G.G. Hoffman, L.L. Haley, M. Daniely, W. Krone, R. Bartrons, U. Kurzik-Dumke, W.K. Lam, I.M. Carr, H. Kehrer-Sawatzki, D.S. Greenspan, Melissa C. Liechty, T.G. Clark, O.A. Ryder, M. Robert-Nicoud, K. Vanhalst, S.J. Charter, D. LaMorticella, M. Minezawa, J.C. Hozier, C. Jolly, E.J. Cartwright, C. M. Carpio, S.E. Antonarakis, J.L. Rosa, H. Götz, A. Paladugu, S. Hoyer-Fender, D.S. Gallagher, F. Mongelard, K. Takahara
المصدر: Cytogenetic and Genome Research. 86:3-20
مصطلحات موضوعية: Genetics, Library science, Biology, Molecular Biology, Genetics (clinical)
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المؤلفون: L. Riesselmann, T. Haaf
المصدر: Cytogenetic and Genome Research. 86:39-42
مصطلحات موضوعية: medicine.medical_specialty, Time Factors, Biology, Chromosomes, S Phase, Genomic Imprinting, Mice, Chromosome Segregation, Chromosome regions, Genetics, medicine, Homologous chromosome, Animals, Molecular Biology, Cells, Cultured, In Situ Hybridization, Fluorescence, Genetics (clinical), S phase, Chromosome 7 (human), medicine.diagnostic_test, Cytogenetics, DNA, Fibroblasts, Molecular biology, Genes, Interphase, DNA Probes, Genomic imprinting, Fluorescence in situ hybridization
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المؤلفون: Marie-Laure Yaspo, Thomas Haaf, R. Lehmann, U. Menzel, Shuichi Asakawa, Dong-Kug Choi, Todd D. Taylor, Jun Kudoh, Kentaro Nagamine, Jean M. Delabar, G. Kauer, Atsushi Toyoda, Tetsushi Yada, Karin Blechschmidt, M. Schillhabel, Gabriele Nordsiek, Yoshiyuki Sakaki, H.-S. Park, David R. Patterson, P. Brant, A. Desario, Alfred Beck, M. Scharfe, Nobuyoshi Shimizu, L. Riesselmann, Yasushi Totoki, O. Schön, Fiona Francis, Kathrin Reichwald, Steffen Hennig, A. Polley, Shinsei Minoshima, J. Reichelt, Susumu Mitsuyama, T. Takagi, Juliane Ramser, Wolfgang Zimmermann, K. Schibuya, A. Schudy, Hidemi Watanabe, Yoram Groner, S. Taudien, Ai Shintani, K. Kumpf, K. Borzym, K. Hornischer, Misao Ohki, Masahira Hattori, K. Gardiner, Emilie Dagand, Eiichi Soeda, Hans Lehrach, Asao Fujiyama, S. Wehrmeyer, H. Blöcker, Richard Reinhardt, Andreas Rump, Sven Klages, Takashi Sasaki, André Rosenthal, Stylianos E. Antonarakis, Dean Nizetic, Kazuhiko Kawasaki, Kazuo Ishii
المصدر: Nature. 407:110-110
مصطلحات موضوعية: Sequence-tagged site, Genetics, Multidisciplinary, DNA codon table, business.industry, Nucleic acid sequence, Medicine, Human genome, P1-derived artificial chromosome, Insertion, Chromosome 21, business, Chromosome 22
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7دورية أكاديمية
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8دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
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9دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
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10دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.
